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Development of a Cancer Nanovaccine to Induce Antigen-specific Immune Responses Based on Large-Sized Porous Silica Nanoparticles.
Shin, Hojeong; Kang, Seounghun; Chae, Se-Youl; Won, Cheolhee; Min, Dal-Hee.
Afiliación
  • Shin H; Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
  • Kang S; Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
  • Chae SY; Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
  • Won C; Institute of Biotherapeutics Convergence Technology, Lemonex Inc., Seoul 06683, Republic of Korea.
  • Min DH; Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
Article en En | MEDLINE | ID: mdl-36913611
ABSTRACT
Cancer vaccine is one of the immunotherapeutic strategies aiming to effectively deliver cancer antigens to professional antigen-presenting cells such as dendritic cells (DCs), macrophages, and B cells to elicit a cancer-specific immune response. Despite the advantages of the cancer vaccine that can be applied to various cancer types, the clinical approach is limited due to the non-specific or adverse immune responses, stability, and safety issues. In this study, we report an injectable nanovaccine platform based on large-sized (∼350 nm) porous silica nanoparticles (PSNs). We found that large-sized PSNs, called PS3, facilitated the formation of an antigen supply depot at the site of injection so that a single injection of PSN-based nanovaccine elicited sufficient tumor-specific cell-mediated and humoral immune response. As a result, antigen-loaded PS3 induced successful tumor regression in prophylactic and therapeutic vaccination.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2023 Tipo del documento: Article